MXPA03010724A - Compuestos de carbamato y oxamida como inhibidores de la produccion de citocina. - Google Patents
Compuestos de carbamato y oxamida como inhibidores de la produccion de citocina.Info
- Publication number
- MXPA03010724A MXPA03010724A MXPA03010724A MXPA03010724A MXPA03010724A MX PA03010724 A MXPA03010724 A MX PA03010724A MX PA03010724 A MXPA03010724 A MX PA03010724A MX PA03010724 A MXPA03010724 A MX PA03010724A MX PA03010724 A MXPA03010724 A MX PA03010724A
- Authority
- MX
- Mexico
- Prior art keywords
- compounds
- carbamate
- inhibitors
- cytokine production
- disclosed
- Prior art date
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- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
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- C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C275/40—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by nitrogen atoms not being part of nitro or nitroso groups
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Abstract
Se describen compuestos aromaticos novedosos de la formula (I) descrita aqui, donde G, E, W, Ar, X, Y y Z son descritos aqui. Los compuestos son utiles para tratar enfermedades o condiciones medidas por citosina como las enfermedades inflamatorias cronicas. Tambien se describen composiciones farmaceuticas que contienen y procesos para producir esos compuestos. Un ejemplo representativo de los compuestos de formula (I) es (a) (ver formula).
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US29360001P | 2001-05-25 | 2001-05-25 | |
PCT/US2002/014400 WO2002096876A1 (en) | 2001-05-25 | 2002-05-08 | Carbamate and oxamide compounds as inhibitors of cytokine production |
Publications (1)
Publication Number | Publication Date |
---|---|
MXPA03010724A true MXPA03010724A (es) | 2004-03-02 |
Family
ID=23129728
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MXPA03010724A MXPA03010724A (es) | 2001-05-25 | 2002-05-08 | Compuestos de carbamato y oxamida como inhibidores de la produccion de citocina. |
Country Status (6)
Country | Link |
---|---|
US (1) | US6743788B2 (es) |
EP (1) | EP1395561A1 (es) |
JP (1) | JP2004531571A (es) |
CA (1) | CA2448626A1 (es) |
MX (1) | MXPA03010724A (es) |
WO (1) | WO2002096876A1 (es) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003072569A1 (en) * | 2002-02-25 | 2003-09-04 | Boehringer Ingelheim Pharmaceuticals, Inc. | 1,4-disubstituted benzofused cycloalkyl urea compounds useful in treating cytokine mediated diseases |
PL377821A1 (pl) * | 2002-11-21 | 2006-02-20 | Chiron Corporation | 2,4,6-tripodstawione pirymidyny jako inhibitory kinazy fosfatydyloinozytolu (PI) 3 i ich zastosowanie w leczeniu nowotworu |
AU2004270733B2 (en) | 2003-09-11 | 2011-05-19 | Itherx Pharma, Inc. | Cytokine inhibitors |
WO2005105757A1 (en) * | 2004-04-22 | 2005-11-10 | The Procter & Gamble Company | Tri-substituted ureas as cytokine inhibitors |
RS53600B1 (en) | 2004-06-17 | 2015-02-27 | Cytokinetics, Inc. | UNITS, PREPARATIONS AND METHODS |
JP2008523072A (ja) | 2004-12-07 | 2008-07-03 | ルーカス ファーマシューティカルズ, インコーポレイテッド | タンパク質キナーゼの阻害剤 |
US7741479B2 (en) | 2004-12-07 | 2010-06-22 | Locus Pharmaceuticals, Inc. | Urea inhibitors of MAP kinases |
US20100016319A1 (en) * | 2005-11-29 | 2010-01-21 | Toray Industries, Inc. A Corporation Of Japan | Arylmethylene urea derivative and use thereof |
EP1959960B1 (en) | 2005-12-15 | 2013-04-10 | Cytokinetics, Inc. | Certain chemical entities, compositions and methods |
EP1962852B1 (en) * | 2005-12-19 | 2017-01-25 | Cytokinetics, Inc. | Compounds, compositions and methods |
JO2660B1 (en) | 2006-01-20 | 2012-06-17 | نوفارتيس ايه جي | Pi-3 inhibitors and methods of use |
US20080064717A1 (en) * | 2006-05-19 | 2008-03-13 | Rajesh Iyengar | Inhibitors of diacylglycerol O-acyltransferase type 1 enzyme |
US20080015227A1 (en) * | 2006-05-19 | 2008-01-17 | Kym Philip R | Inhibitors of diacylglycerol O-acyltransferase type 1 enzyme |
ES2381895T3 (es) * | 2007-02-06 | 2012-06-01 | Novartis Ag | Inhibidores de PI 3-quinasa y métodos para su uso |
RU2010115747A (ru) * | 2007-09-21 | 2011-10-27 | Санофи-Авентис (Fr) | (циклопропилфенил)фенилоксаламиды, способ их получения и их применения в качестве лекарственного средства |
MX2010002461A (es) * | 2007-09-21 | 2010-03-26 | Sanofi Aventis | (carboxilalquilenfenil)feniloxamidas, metodo para su produccion y uso de las mismas como medicamento. |
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ES2665619T3 (es) | 2013-03-14 | 2018-04-26 | Novartis Ag | 3-Pirimidin-4-il-oxazolidin-2-onas como inhibidores de IDH mutante |
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CN106748990A (zh) * | 2016-11-14 | 2017-05-31 | 西安交通大学 | 一种具有抗肿瘤活性的双芳基脲类化合物及其制备方法和应用 |
CN106748989B (zh) * | 2016-11-14 | 2020-03-17 | 西安交通大学 | 一种具有抗肿瘤活性的二芳基脲类化合物及其制备方法和应用 |
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TW202112767A (zh) | 2019-06-17 | 2021-04-01 | 美商佩特拉製藥公司 | 作為磷脂酸肌醇磷酸激酶抑制劑之胺基吡啶衍生物 |
US11596612B1 (en) | 2022-03-08 | 2023-03-07 | PTC Innovations, LLC | Topical anesthetics |
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HU185294B (en) | 1980-12-29 | 1984-12-28 | Chinoin Gyogyszer Es Vegyeszet | Process for producing substituted urea derivatives |
GB8908869D0 (en) | 1989-04-19 | 1989-06-07 | Shell Int Research | A process for the preparation of aromatic ureas |
WO1991004027A1 (en) | 1989-09-15 | 1991-04-04 | Pfizer Inc. | New n-aryl and n-heteroarylamide and urea derivatives as inhibitors of acyl coenzyme a: cholesterol acyl transferase (acat) |
RU94046149A (ru) | 1992-05-28 | 1996-11-27 | Пфайзер Инк. (US) | Новые n-арил и n-гетероарил производные мочевины как ингибиторы ацил кофермента а:холестерин ацил трансферазы (асат) фармацевтическая композиция, способ ингибирования (асат) |
GB9302275D0 (en) | 1993-02-05 | 1993-03-24 | Smithkline Beecham Plc | Novel compounds |
JPH11514651A (ja) | 1995-10-31 | 1999-12-14 | メルク エンド カンパニー インコーポレーテッド | 置換ピリジルピロール、前記化合物を含む組成物及び使用方法 |
US6211373B1 (en) | 1996-03-20 | 2001-04-03 | Smithkline Beecham Corporation | Phenyl urea antagonists of the IL-8 receptor |
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ES2151467T3 (es) | 1997-05-23 | 2005-03-01 | Bayer Corporation | Arilureas para el tratamiento de enfermedades inflamatorias o inmunomoduladoras. |
WO1999032111A1 (en) | 1997-12-22 | 1999-07-01 | Bayer Corporation | INHIBITION OF p38 KINASE ACTIVITY USING SUBSTITUTED HETEROCYCLIC UREAS |
TR200100917T2 (tr) | 1997-12-22 | 2001-07-23 | Bayer Corporation | Aril ve heteroaril sübstitüentli heteroksiklik üreler kullanılarak RAF kinazın inhibe edilmesi |
AU1939999A (en) | 1997-12-22 | 1999-07-12 | Bayer Corporation | Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas |
ATE346600T1 (de) | 1997-12-22 | 2006-12-15 | Bayer Pharmaceuticals Corp | Inhibierung der p38 kinase-aktivität durch die verwendung von aryl- und heteroarylsubstituierten harnstoffen |
RU2232015C2 (ru) | 1997-12-22 | 2004-07-10 | Байер Копэрейшн | Способ подавления роста опухолевых клеток, опосредованного киназой raf, гетероциклические производные мочевины (варианты), фармацевтическая композиция (варианты) |
TR200100840T2 (tr) * | 1998-09-25 | 2001-10-22 | Astrazeneca Ab | Benzamid türevleri ve bunların sitokin inhibe edicileri olarak kullanımı |
UA73492C2 (en) | 1999-01-19 | 2005-08-15 | Aromatic heterocyclic compounds as antiinflammatory agents | |
SK12832001A3 (sk) * | 1999-03-12 | 2002-01-07 | Boehringer Ingelheim Pharmaceuticals, Inc. | Protizápalové látky, spôsob ich výroby, farmaceutický prostriedok s ich obsahom a ich použitie |
EP1163236B1 (en) | 1999-03-12 | 2005-11-09 | Boehringer Ingelheim Pharmaceuticals Inc. | Aromatic heterocyclic compounds as anti-inflammatory agents |
MXPA02004879A (es) * | 1999-11-16 | 2002-08-30 | Boehringer Ingelheim Pharma | Derivados de urea como agentes antiinflamatorios. |
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- 2002-05-08 WO PCT/US2002/014400 patent/WO2002096876A1/en not_active Application Discontinuation
- 2002-05-08 CA CA002448626A patent/CA2448626A1/en not_active Abandoned
- 2002-05-08 JP JP2003500056A patent/JP2004531571A/ja active Pending
- 2002-05-08 EP EP02731697A patent/EP1395561A1/en not_active Withdrawn
- 2002-05-17 US US10/147,675 patent/US6743788B2/en not_active Expired - Lifetime
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US20030092702A1 (en) | 2003-05-15 |
WO2002096876A1 (en) | 2002-12-05 |
JP2004531571A (ja) | 2004-10-14 |
US6743788B2 (en) | 2004-06-01 |
EP1395561A1 (en) | 2004-03-10 |
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